Clinical Research Jobs in Czech Republic

Responsible for coordinating the operational and strategic aspects for Clinical Trial SubmissionsEssential Functions:Lead the clinical trial submission process from strategy development through to regulatory approval.Develop plan and coordinate submission strategies to ensure timely and successful t...

Job OverviewAssociate Clinical Project Management Directors supervise manage and provide oversight to assigned Clinical Project Management staff who manage or support studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction. Man...

Advance AbbVies pipeline by striving for excellence in clinical research turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance.Partners with the investigator and site staff for meaningful and effective engagements positioning Ab...

The Senior Specialist Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness. The role provides subject matter expertise ensures regulatory compliance and serves as a key liaison between internal teams clients and external stakeholde...

Due to the continued growth of our Global Study Start Up Group we are now seeking a Site Contracts Manager who will be responsible for overseeing the negotiation process of clinical study agreements on assigned trials and who will act as a subject matter expert to our sponsors and stakeholders in ow...

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will b...

Assists with set up and maintenance of the Trial Master File (TMF). Serves as main point of contact for all TMF-related activities for assigned projects. Processing and indexing of project documents for the TMF in accordance with project-specific guidelines and relevant SOPs. Upon study closure assi...

The EDC Developer within the ERGOMED Data Management (DM) department is responsible for all tasks linked to the building of the EDC application for complex projects. The EDC Developer represents a position under direction of the Director of Data Management with oversight by the Project Data Manager...

Position SummaryResponsible for the management of the end-to-end investigator/site payment processes including payment calculations creation and management of purchase orders and clinical trial payments. Acts as liaison among colleagues within Contract & Centralized Services other GCO teams and Site...

The EDC Developer within the ERGOMED Data Management (DM) department is responsible for all tasks linked to the building of the EDC application for complex projects. The EDC Developer represents a position under direction of the Director of Data Management with oversight by the Project Data Manager...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations standard operating procedures (SOPs) project requirements and contractual/budgetary guidelines. May also include maintenance activities.Op...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate (Level II) Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials acr...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsSome degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Standing for full shift Will work with hazardous/toxic materialsJob DescriptionJoin Us as a Supervisor Clinical Research Nursing...

DescriptionWho we are:Spire Orthopedic Partners is a growing national partnership of orthopedic practices that provides the support capital and operational resources physicians need to grow thriving practices for the future. As a Management Services Organization (MSO) Spire provides the infrastructu...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Clinical Research Associate I Make an Impact at the Forefront of InnovationWe have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs spanning 2700 clinical trials across 100 c...

Join Our Team and Shape the Future of Clinical Research!At Fortrea we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist you will play a critical role in negotiating and managing site agreements confidentiality agreem...

Shape HR Strategy at the Heart of Global Drug Safety At ERGOMED Group our pharmacovigilance teams protect patients around the world and were looking for a Global HR Business Partner who wants to do the same for our people. This is a rare opportunity to sit at the intersection of HR strategy and one...

Job OverviewThis role works closely with the Global Market Insights (GMI) and OneKey leadership team in managing operations initiatives and contributing to the improvement of business processes (forecasting opportunity pipeline management CRM administration/training project management reporting and...

Project Leads are an integral part of clinical trial delivery liaising with clinical teams to improve patients lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual r...

At IQVIA our Clinical Leads play a critical role in bringing new medicines to patients faster. As part of the Global Study Leadership team youll lead the clinical delivery of international studies partnering with Project Leads and cross-functional teams to ensure projects are delivered with quality...